Canonical Allele Identifier: CA2639095985
Gene: CA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.60149937G>A , CM000679.2:g.60149937G>A GRCh38
NC_000017.10:g.58227298G>A , CM000679.1:g.58227298G>A GRCh37
NC_000017.9:g.55582080G>A NCBI36
NG_012050.1:g.4997G>A
NG_012050.2:g.4997G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300900.8:c.-98G>A ENSP00000300900.3:n.-98G>A
NM_000717.4:c.-98G>A NP_000708.1:n.-98G>A
NR_137422.1:n.2G>A