Canonical Allele Identifier: CA16956841
Gene:

Linked Data

dbSNP Id: rs1555791
gnomAD v3: 1-2567423-G-T
gnomAD v4: 1-2567423-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567423G>T , CM000663.2:g.2567423G>T GRCh38
NC_000001.10:g.2498862G>T , CM000663.1:g.2498862G>T GRCh37
NC_000001.9:g.2475556C>A NCBI36
NG_047096.1:g.16059G>T

Transcript Alleles

HGVS Amino-acid change
NR_121638.1:n.71+818G>T