Canonical Allele Identifier: CA214412866

Gene:

Linked Data

• dbSNP Id: rs547330600
• MyVariant Identifiers: chr10:g.124217605C>A (hg19) ; chr10:g.122458089C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458089C>A , CM000672.2:g.122458089C>A	GRCh38
NC_000010.10:g.124217605C>A , CM000672.1:g.124217605C>A	GRCh37
NC_000010.9:g.124207595C>A	NCBI36
NG_011554.1:g.1565C>A
NG_011725.1:g.8427C>A

Transcript Alleles

HGVS	Amino-acid change
XR_946382.1:n.1827+406G>T
XR_946383.1:n.1827+406G>T
XR_946384.1:n.1576+406G>T
XR_946385.1:n.1827+406G>T
XR_946382.2:n.1855+406G>T
XR_946383.2:n.1855+406G>T
XR_946384.2:n.1580+406G>T
XR_946385.2:n.1855+406G>T