Canonical Allele Identifier: CA307575818

Gene:

Linked Data

• dbSNP Id: rs896839472
• gnomAD v3: 19-33521939-G-C
• gnomAD v4: 19-33521939-G-C
• MyVariant Identifiers: chr19:g.34012845G>C (hg19) ; chr19:g.33521939G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521939G>C , CM000681.2:g.33521939G>C	GRCh38
NC_000019.9:g.34012845G>C , CM000681.1:g.34012845G>C	GRCh37
NC_000019.8:g.38704685G>C	NCBI36
NG_013358.1:g.4955C>G
NG_013358.2:g.4955C>G

Transcript Alleles

HGVS	Amino-acid Change
XR_001754035.2:n.6G>C
XR_935918.2:n.6G>C