Canonical Allele Identifier: CA881156481

Gene:

Linked Data

• dbSNP Id: rs1390731213
• gnomAD v3: 19-28544815-C-T
• gnomAD v4: 19-28544815-C-T
• MyVariant Identifiers: chr19:g.29035722C>T (hg19) ; chr19:g.28544815C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.28544815C>T , CM000681.2:g.28544815C>T	GRCh38
NC_000019.9:g.29035722C>T , CM000681.1:g.29035722C>T	GRCh37
NC_000019.8:g.33727562C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110759.1:n.657-78035G>A
XR_243979.1:n.110-51792G>A