Canonical Allele Identifier: CA54579256
Gene:

Linked Data

dbSNP Id: rs903326828
MyVariant Identifiers: chr2:g.118079636A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079636A>C , CM000664.2:g.118079636A>C GRCh38
NC_000002.11:g.118837212A>C , CM000664.1:g.118837212A>C GRCh37
NC_000002.10:g.118553682A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2104T>G XP_011510607.1:n.697-2104T>G
XR_001739662.2:n.138+8615T>G