Canonical Allele Identifier: CA2748612080

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1554160T>C , CM000664.2:g.1554160T>C	GRCh38
NC_000002.11:g.1557932T>C , CM000664.1:g.1557932T>C	GRCh37
NC_000002.10:g.1536939T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011510447.1:c.-1013T>C	XP_011508749.1:n.-1013T>C
XM_011510448.1:c.-1013T>C	XP_011508750.1:n.-1013T>C
XR_922720.1:n.85+2338A>G
XM_017005455.1:c.-1013T>C	XP_016860944.1:n.-1013T>C
NR_168373.1:n.746-10T>C