Canonical Allele Identifier: CA59107106
Gene:

Linked Data

dbSNP Id: rs550432119
gnomAD v3: 2-155870770-C-G
gnomAD v4: 2-155870770-C-G
MyVariant Identifiers: chr2:g.156727282C>G (hg19) chr2:g.155870770C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870770C>G , CM000664.2:g.155870770C>G GRCh38
NC_000002.11:g.156727282C>G , CM000664.1:g.156727282C>G GRCh37
NC_000002.10:g.156435528C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3583G>C
XR_001739749.1:n.331-29786G>C
XR_001739750.1:n.331-29786G>C
XR_001739751.1:n.331-29786G>C
XR_923501.2:n.331-3583G>C
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