Canonical Allele Identifier: CA1087465302
Gene:

Linked Data

dbSNP Id: rs1761796650
gnomAD v4: 6-31440121-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440121C>A , CM000668.2:g.31440121C>A GRCh38
NC_000006.11:g.31407898C>A , CM000668.1:g.31407898C>A GRCh37
NC_000006.10:g.31515877C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-69G>T
Search 100 bp 5'
Search 100 bp 3'