Canonical Allele Identifier: CA1827744214
Gene:

Linked Data

dbSNP Id: rs996121117
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787426G>T , CM000671.2:g.1787426G>T GRCh38
NC_000009.11:g.1787426G>T , CM000671.1:g.1787426G>T GRCh37
NC_000009.10:g.1777426G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68514G>T
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Search 100 bp 3'