Canonical Allele Identifier: CA1094718396

Gene:

Linked Data

• dbSNP Id: rs1774560513
• gnomAD v3: 6-134398908-A-T
• gnomAD v4: 6-134398908-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.134398908A>T , CM000668.2:g.134398908A>T	GRCh38
NC_000006.11:g.134720046A>T , CM000668.1:g.134720046A>T	GRCh37
NC_000006.10:g.134761739A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428023.2:n.23+179A>T