Canonical Allele Identifier: CA59107047
Gene:

Linked Data

dbSNP Id: rs977391258
MyVariant Identifiers: chr2:g.155870270G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870270G>C , CM000664.2:g.155870270G>C GRCh38
NC_000002.11:g.156726782G>C , CM000664.1:g.156726782G>C GRCh37
NC_000002.10:g.156435028G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3083C>G
XR_001739749.1:n.331-29286C>G
XR_001739750.1:n.331-29286C>G
XR_001739751.1:n.331-29286C>G
XR_923501.2:n.331-3083C>G