LDH info

Canonical Allele Identifier: CA126963
Gene: CYP2C19 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16899
ClinVar RCV Id: RCV000018397 RCV000018398 RCV000211151 RCV000291495 RCV000782441 RCV000782449 RCV000782521 RCV000782522 RCV000782523 RCV000782524 RCV000782525 RCV000782526 RCV000782527 RCV000782528 RCV000782645 RCV000782646 RCV000782647 RCV000782648 RCV000782649 RCV000782693 RCV000782694 RCV000782707 RCV000782708 RCV000782709 RCV000782710 RCV000782711 RCV000782712 RCV000782713 RCV000782714 RCV000782715 RCV000782952 RCV000782953 RCV000782954 RCV000782955 RCV000782956 RCV000782957 RCV000782958 RCV000782959 RCV000783068 RCV000783084 RCV000783085 RCV000783086 RCV000783087 RCV000783088 RCV000783089 RCV000783147 RCV000783148 RCV000783149 RCV000783179 RCV000783180 RCV000783181 RCV000783302 RCV000783303 RCV000783304 RCV000783305 RCV000783306 RCV000783307 RCV000783308 RCV000783309 RCV000783449 RCV000783450 RCV000783451 RCV000783452 RCV000783453 RCV000783454 RCV000783503 RCV000783519 RCV000783520 RCV000783521 RCV000783579 RCV000783580 RCV000783581 RCV000783582 RCV000783583 RCV000783584 RCV000783614 RCV000783621 RCV000783622 RCV000783623 RCV000783624 RCV000783625 RCV000783626 RCV000783656 RCV000783667 RCV000783674 RCV000783675 RCV000783676 RCV000783677 RCV000783678 RCV000783679 RCV000783680 RCV000783717 RCV000783718 RCV000783749 RCV000783750 RCV000783751 RCV000783752 RCV000783877 RCV000783878 RCV000783879 RCV000783880 RCV000783881 RCV000783882 RCV000783883 RCV000783937 RCV000783938 RCV000783939 RCV000783940 RCV000783941 RCV000783942 RCV000783943 RCV000783944 RCV000783945 RCV000783946 RCV000783947 RCV000784182 RCV000784183 RCV000784184 RCV000784185 RCV000784186 RCV000784187 RCV000784188 RCV000784189 RCV000784190 RCV000784191 RCV000784192 RCV000784193 RCV000784382 RCV000784383 RCV000784384 RCV000784406 RCV000784410 RCV000784411 RCV000784412 RCV000784413 RCV000784414 RCV000784415 RCV000784416 RCV000784539 RCV000784540 RCV000784688 RCV000784689 RCV000784690 RCV000784691 RCV000784753 RCV000784754 RCV000784755 RCV000784845 RCV000784846 RCV000784847 RCV000784848
dbSNP Id: rs4986893

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780653G>A , CM000672.2:g.94780653G>A GRCh38
NC_000010.10:g.96540410G>A , CM000672.1:g.96540410G>A GRCh37
NC_000010.9:g.96530400G>A NCBI36
NG_008384.2:g.22948G>A
NG_008384.3:g.22973G>A

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.636G>A VV NP_000760.1:p.Trp212Ter
NM_000769.4:c.636G>A VV MANE Preferred NP_000760.1:p.Trp212Ter
ENST00000371321.7:c.636G>A ENSP00000360372.3:p.Trp212Ter
ENST00000464755.1:n.1399G>A ENSP00000483243.1:p.=