Canonical Allele Identifier: CA1116942019
Gene:

Linked Data

dbSNP Id: rs1810398000
gnomAD v3: 8-97269624-A-C
gnomAD v4: 8-97269624-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269624A>C , CM000670.2:g.97269624A>C GRCh38
NC_000008.10:g.98281852A>C , CM000670.1:g.98281852A>C GRCh37
NC_000008.9:g.98351028A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149446T>G