Canonical Allele Identifier: CA214412847

Gene:

Linked Data

• dbSNP Id: rs953633456
• gnomAD v3: 10-122458053-C-A
• gnomAD v4: 10-122458053-C-A
• MyVariant Identifiers: chr10:g.124217569C>A (hg19) ; chr10:g.122458053C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458053C>A , CM000672.2:g.122458053C>A	GRCh38
NC_000010.10:g.124217569C>A , CM000672.1:g.124217569C>A	GRCh37
NC_000010.9:g.124207559C>A	NCBI36
NG_011554.1:g.1529C>A
NG_011725.1:g.8391C>A

Transcript Alleles

HGVS	Amino-acid change
XR_946382.1:n.1827+442G>T
XR_946383.1:n.1827+442G>T
XR_946384.1:n.1576+442G>T
XR_946385.1:n.1827+442G>T
XR_946382.2:n.1855+442G>T
XR_946383.2:n.1855+442G>T
XR_946384.2:n.1580+442G>T
XR_946385.2:n.1855+442G>T