Canonical Allele Identifier: CA1157252196
Gene:

Linked Data

dbSNP Id: rs4654903
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19874497A>T , CM000663.2:g.19874497A>T GRCh38
NC_000001.10:g.20200990A>T , CM000663.1:g.20200990A>T GRCh37
NC_000001.9:g.20073577A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947027.1:n.266-8745T>A
XR_947028.1:n.266-8745T>A
XR_947027.2:n.167-8745T>A
XR_947028.2:n.167-8745T>A
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