Canonical Allele Identifier: CA660863745

Gene:

Linked Data

• dbSNP Id: rs776882172
• MyVariant Identifiers: chr10:g.124217923G>T (hg19) ; chr10:g.122458407G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458407G>T , CM000672.2:g.122458407G>T	GRCh38
NC_000010.10:g.124217923G>T , CM000672.1:g.124217923G>T	GRCh37
NC_000010.9:g.124207913G>T	NCBI36
NG_011554.1:g.1883G>T
NG_011725.1:g.8745G>T

Transcript Alleles

HGVS	Amino-acid Change
XR_946382.1:n.1827+88C>A
XR_946383.1:n.1827+88C>A
XR_946384.1:n.1576+88C>A
XR_946385.1:n.1827+88C>A
XR_946382.2:n.1855+88C>A
XR_946383.2:n.1855+88C>A
XR_946384.2:n.1580+88C>A
XR_946385.2:n.1855+88C>A