Canonical Allele Identifier: CA660863602

Gene:

Linked Data

• dbSNP Id: rs1000298854
• MyVariant Identifiers: chr10:g.124217609G>C (hg19) ; chr10:g.122458093G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458093G>C , CM000672.2:g.122458093G>C	GRCh38
NC_000010.10:g.124217609G>C , CM000672.1:g.124217609G>C	GRCh37
NC_000010.9:g.124207599G>C	NCBI36
NG_011554.1:g.1569G>C
NG_011725.1:g.8431G>C

Transcript Alleles

HGVS	Amino-acid change
XR_946382.1:n.1827+402C>G
XR_946383.1:n.1827+402C>G
XR_946384.1:n.1576+402C>G
XR_946385.1:n.1827+402C>G
XR_946382.2:n.1855+402C>G
XR_946383.2:n.1855+402C>G
XR_946384.2:n.1580+402C>G
XR_946385.2:n.1855+402C>G