Canonical Allele Identifier: CA560796658
Gene:

Linked Data

dbSNP Id: rs907497952
gnomAD v2: 5-91518642-A-C
gnomAD v3: 5-92222825-A-C
gnomAD v4: 5-92222825-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222825A>C , CM000667.2:g.92222825A>C GRCh38
NC_000005.9:g.91518642A>C , CM000667.1:g.91518642A>C GRCh37
NC_000005.8:g.91554398A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18141A>C