Canonical Allele Identifier: CA59107041
Gene:

Linked Data

dbSNP Id: rs1008224198
gnomAD v2: 2-156726716-C-G
gnomAD v3: 2-155870204-C-G
gnomAD v4: 2-155870204-C-G
MyVariant Identifiers: chr2:g.156726716C>G (hg19) chr2:g.155870204C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870204C>G , CM000664.2:g.155870204C>G GRCh38
NC_000002.11:g.156726716C>G , CM000664.1:g.156726716C>G GRCh37
NC_000002.10:g.156434962C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3017G>C
XR_001739749.1:n.331-29220G>C
XR_001739750.1:n.331-29220G>C
XR_001739751.1:n.331-29220G>C
XR_923501.2:n.331-3017G>C
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