Canonical Allele Identifier: CA51761766
Gene:

Linked Data

dbSNP Id: rs1003485774
MyVariant Identifiers: chr2:g.81872928A>C (hg19) chr2:g.81645804A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.81645804A>C , CM000664.2:g.81645804A>C GRCh38
NC_000002.11:g.81872928A>C , CM000664.1:g.81872928A>C GRCh37
NC_000002.10:g.81726439A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940294.1:n.563+66195A>C
XR_940295.1:n.485+97057A>C
XR_001739571.1:n.485+97057A>C
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