Canonical Allele Identifier: CA310850294
Gene:

Linked Data

dbSNP Id: rs879445432
gnomAD v2: 20-2451636-C-G
gnomAD v3: 20-2470990-C-G
gnomAD v4: 20-2470990-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470990C>G , CM000682.2:g.2470990C>G GRCh38
NC_000020.10:g.2451636C>G , CM000682.1:g.2451636C>G GRCh37
NC_000020.9:g.2399636C>G NCBI36
NG_042057.1:g.4864G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3232G>C ENSP00000456213.1:n.305-3232G>C