Canonical Allele Identifier: CA1157252223
Gene:

Linked Data

dbSNP Id: rs2045189789
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19874527C>T , CM000663.2:g.19874527C>T GRCh38
NC_000001.10:g.20201020C>T , CM000663.1:g.20201020C>T GRCh37
NC_000001.9:g.20073607C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947027.1:n.266-8775G>A
XR_947028.1:n.266-8775G>A
XR_947027.2:n.167-8775G>A
XR_947028.2:n.167-8775G>A
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