Canonical Allele Identifier: CA2580620033
Gene:

Linked Data

gnomAD v4: 20-2470857-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470857G>C , CM000682.2:g.2470857G>C GRCh38
NC_000020.10:g.2451503G>C , CM000682.1:g.2451503G>C GRCh37
NC_000020.9:g.2399503G>C NCBI36
NG_042057.1:g.4997C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3099C>G ENSP00000456213.1:n.305-3099C>G