Canonical Allele Identifier: CA1157252130
Gene:

Linked Data

dbSNP Id: rs2045189032
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19874460A>G , CM000663.2:g.19874460A>G GRCh38
NC_000001.10:g.20200953A>G , CM000663.1:g.20200953A>G GRCh37
NC_000001.9:g.20073540A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947027.1:n.266-8708T>C
XR_947028.1:n.266-8708T>C
XR_947027.2:n.167-8708T>C
XR_947028.2:n.167-8708T>C
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