Canonical Allele Identifier: CA542918787

Gene:

Linked Data

• dbSNP Id: rs1158336116
• gnomAD v2: 3-53090986-G-A
• gnomAD v3: 3-53056970-G-A
• gnomAD v4: 3-53056970-G-A
• MyVariant Identifiers: chr3:g.53090986G>A (hg19) ; chr3:g.53056970G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53056970G>A , CM000665.2:g.53056970G>A	GRCh38
NC_000003.11:g.53090986G>A , CM000665.1:g.53090986G>A	GRCh37
NC_000003.10:g.53066026G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607203.1:c.318-9731C>T
ENST00000607283.5:c.465-13716C>T
ENST00000607495.5:c.447+20718C>T