Canonical Allele Identifier: CA10838634
Gene:

Linked Data

dbSNP Id: rs947008
gnomAD v2: 1-56727884-T-C
gnomAD v3: 1-56262212-T-C
gnomAD v4: 1-56262212-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262212T>C , CM000663.2:g.56262212T>C GRCh38
NC_000001.10:g.56727884T>C , CM000663.1:g.56727884T>C GRCh37
NC_000001.9:g.56500472T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641109.1:c.760-13012A>G ENSP00000493138.1:n.760-13012A>G
ENST00000641346.1:c.367-13012A>G
ENST00000641415.1:c.193-8319A>G
ENST00000641494.1:c.379-13012A>G
ENST00000642129.1:c.769-13012A>G