Canonical Allele Identifier: CA1839056679
Gene:

Linked Data

dbSNP Id: rs568120540
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755975G>T , CM000671.2:g.21755975G>T GRCh38
NC_000009.11:g.21755974G>T , CM000671.1:g.21755974G>T GRCh37
NC_000009.10:g.21745974G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11850C>A
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