Canonical Allele Identifier: CA2424797245
Gene:

Linked Data

dbSNP Id: rs56156506

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38140399A>C , CM000685.2:g.38140399A>C GRCh38
NC_000023.10:g.37999652A>C , CM000685.1:g.37999652A>C GRCh37
NC_000023.9:g.37884596A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000465127.1:c.172-525722A>C ENSP00000417050.1:n.172-525722A>C