Canonical Allele Identifier: CA2657649551

Gene:

Linked Data

• gnomAD v4: 2-1554060-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1554060C>A , CM000664.2:g.1554060C>A	GRCh38
NC_000002.11:g.1557832C>A , CM000664.1:g.1557832C>A	GRCh37
NC_000002.10:g.1536839C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011510447.1:c.-1113C>A	XP_011508749.1:n.-1113C>A
XM_011510448.1:c.-1113C>A	XP_011508750.1:n.-1113C>A
XR_922720.1:n.85+2438G>T
XM_017005455.1:c.-1113C>A	XP_016860944.1:n.-1113C>A
NR_168373.1:n.746-110C>A