Canonical Allele Identifier: CA214412966

Gene:

Linked Data

• dbSNP Id: rs553903178
• MyVariant Identifiers: chr10:g.124217735T>C (hg19) ; chr10:g.122458219T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458219T>C , CM000672.2:g.122458219T>C	GRCh38
NC_000010.10:g.124217735T>C , CM000672.1:g.124217735T>C	GRCh37
NC_000010.9:g.124207725T>C	NCBI36
NG_011554.1:g.1695T>C
NG_011725.1:g.8557T>C

Transcript Alleles

HGVS	Amino-acid Change
XR_946382.1:n.1827+276A>G
XR_946383.1:n.1827+276A>G
XR_946384.1:n.1576+276A>G
XR_946385.1:n.1827+276A>G
XR_946382.2:n.1855+276A>G
XR_946383.2:n.1855+276A>G
XR_946384.2:n.1580+276A>G
XR_946385.2:n.1855+276A>G