Canonical Allele Identifier: CA198806
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 44729
dbSNP Id: rs111033293

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20189581T>C , CM000675.2:g.20189581T>C GRCh38
NC_000013.9:g.19661720T>C NCBI36
NC_000013.10:g.20763720T>C , CM000675.1:g.20763720T>C GRCh37
NG_008358.1:g.8395A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.1:c.1A>G
ENST00000382848.4:c.1A>G
NM_004004.5:c.1A>G
XM_011535049.1:c.1A>G