Canonical Allele Identifier: CA915282695
Gene:

Linked Data

gnomAD v2: 6-31407562-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439785C>T , CM000668.2:g.31439785C>T GRCh38
NC_000006.11:g.31407562C>T , CM000668.1:g.31407562C>T GRCh37
NC_000006.10:g.31515541C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.322G>A
Search 100 bp 5'
Search 100 bp 3'