Canonical Allele Identifier: CA2611998999
Gene:

Linked Data

gnomAD v4: 11-2444544-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444544T>C , CM000673.2:g.2444544T>C GRCh38
NC_000011.9:g.2465774T>C , CM000673.1:g.2465774T>C GRCh37
NC_000011.8:g.2422350T>C NCBI36
NG_008935.1:g.4554T>C , LRG_287:g.4554T>C

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.27A>G