Canonical Allele Identifier: CA759294235
Gene:

Linked Data

dbSNP Id: rs1161000455
gnomAD v3: 2-155870192-C-T
gnomAD v4: 2-155870192-C-T
MyVariant Identifiers: chr2:g.156726704C>T (hg19) chr2:g.155870192C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870192C>T , CM000664.2:g.155870192C>T GRCh38
NC_000002.11:g.156726704C>T , CM000664.1:g.156726704C>T GRCh37
NC_000002.10:g.156434950C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3005G>A
XR_001739749.1:n.331-29208G>A
XR_001739750.1:n.331-29208G>A
XR_001739751.1:n.331-29208G>A
XR_923501.2:n.331-3005G>A
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