Canonical Allele Identifier: CA1139443614
Gene:

Linked Data

dbSNP Id: rs2043466117
gnomAD v3: Y-15311385-T-A
gnomAD v4: Y-15311385-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15311385T>A , CM000686.2:g.15311385T>A GRCh38
NC_000024.9:g.17423265T>A , CM000686.1:g.17423265T>A GRCh37
NC_000024.8:g.15932659T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001756089.1:n.309+37284A>T