Canonical Allele Identifier: CA2610264823
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781794_94781795insAAGCA , CM000672.2:g.94781794_94781795insAAGCA GRCh38
NC_000010.10:g.96541551_96541552insAAGCA , CM000672.1:g.96541551_96541552insAAGCA GRCh37
NC_000010.9:g.96531541_96531542insAAGCA NCBI36
NG_008384.2:g.24089_24090insAAGCA
NG_008384.3:g.24114_24115insAAGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.643-27_643-26insAAGCA MANE Select ENSP00000360372.3:n.643-27_643-26insAAGCA...
ENST00000645461.1:n.1696-27_1696-26insAAGCA
ENST00000371321.7:c.643-27_643-26insAAGCA ENSP00000360372.3:n.643-27_643-26insAAGCA...
ENST00000464755.1:c.1406-27_1406-26insAAGCA ENSP00000483243.1:n.1406-27_1406-26insAAG...
NM_000769.2:c.643-27_643-26insAAGCA NP_000760.1:n.643-27_643-26insAAGCA
NM_000769.4:c.643-27_643-26insAAGCA MANE Select NP_000760.1:n.643-27_643-26insAAGCA