Canonical Allele Identifier: CA2346122806
Gene:

Linked Data

dbSNP Id: rs965288201
gnomAD v4: 20-2470999-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470999A>C , CM000682.2:g.2470999A>C GRCh38
NC_000020.10:g.2451645A>C , CM000682.1:g.2451645A>C GRCh37
NC_000020.9:g.2399645A>C NCBI36
NG_042057.1:g.4855T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3241T>G ENSP00000456213.1:n.305-3241T>G