Canonical Allele Identifier: CA2639095986
Gene: CA4 HGNC NCBI

Linked Data

gnomAD v4: 17-60149937-G-T
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Genomic Alleles

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

Transcript Alleles

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