Canonical Allele Identifier: CA338567942
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759982
ClinVar RCV Id: RCV002396400
dbSNP Id: rs1570786774
MyVariant Identifiers: chr1:g.15772216T>G (hg19) chr1:g.15445721T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445721T>G , CM000663.2:g.15445721T>G GRCh38
NC_000001.10:g.15772216T>G , CM000663.1:g.15772216T>G GRCh37
NC_000001.9:g.15644803T>G NCBI36
NG_009253.1:g.12279T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.764T>G MANE Select ENSP00000365116.4:p.Val255Gly
ENST00000375943.6:c.*218T>G ENSP00000365110.2:n.*218T>G
ENST00000375949.4:c.764T>G ENSP00000365116.4:p.Val255Gly
ENST00000483406.1:n.528T>G
NM_007272.2:c.764T>G NP_009203.2:p.Val255Gly
XM_011540550.1:c.618T>G XP_011538852.1:p.Gly206=
NM_007272.3:c.764T>G MANE Select NP_009203.2:p.Val255Gly
Search 100 bp 5'
Search 100 bp 3'