Canonical Allele Identifier: CA337624575
Gene:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8665694G>A , CM000686.2:g.8665694G>A GRCh38
NC_000024.9:g.8533735G>A , CM000686.1:g.8533735G>A GRCh37
NC_000024.8:g.8593735G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624593.1:c.-56-7004C>T ENSP00000485106.1:n.-56-7004C>T