Canonical Allele Identifier: CA2651630688
Gene:

Linked Data

gnomAD v4: 20-2470894-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470894C>A , CM000682.2:g.2470894C>A GRCh38
NC_000020.10:g.2451540C>A , CM000682.1:g.2451540C>A GRCh37
NC_000020.9:g.2399540C>A NCBI36
NG_042057.1:g.4960G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3136G>T ENSP00000456213.1:n.305-3136G>T