Canonical Allele Identifier: CA569191046
Gene:

Linked Data

dbSNP Id: rs1451716845
gnomAD v2: 6-98550338-A-T
gnomAD v3: 6-98102462-A-T
gnomAD v4: 6-98102462-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102462A>T , CM000668.2:g.98102462A>T GRCh38
NC_000006.11:g.98550338A>T , CM000668.1:g.98550338A>T GRCh37
NC_000006.10:g.98657059A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3192A>T
XR_942809.1:n.456+3192A>T