Canonical Allele Identifier: CA2664003138

Gene:

Linked Data

• gnomAD v4: 2-240868477-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868477G>T , CM000664.2:g.240868477G>T	GRCh38
NC_000002.11:g.241807894G>T , CM000664.1:g.241807894G>T	GRCh37
NC_000002.10:g.241456567G>T	NCBI36
NG_008005.1:g.4733G>T

Transcript Alleles

HGVS	Amino-acid Change
XR_924060.1:n.405+1756C>A