Canonical Allele Identifier: CA59107060
Gene:

Linked Data

dbSNP Id: rs547772115
gnomAD v2: 2-156726866-A-G
gnomAD v3: 2-155870354-A-G
gnomAD v4: 2-155870354-A-G
MyVariant Identifiers: chr2:g.156726866A>G (hg19) chr2:g.155870354A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870354A>G , CM000664.2:g.155870354A>G GRCh38
NC_000002.11:g.156726866A>G , CM000664.1:g.156726866A>G GRCh37
NC_000002.10:g.156435112A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3167T>C
XR_001739749.1:n.331-29370T>C
XR_001739750.1:n.331-29370T>C
XR_001739751.1:n.331-29370T>C
XR_923501.2:n.331-3167T>C
Search 100 bp 5'
Search 100 bp 3'