Canonical Allele Identifier: CA292199813
Gene: CA4 HGNC NCBI

Linked Data

dbSNP Id: rs915691626
gnomAD v2: 17-58227297-G-C
gnomAD v3: 17-60149936-G-C
gnomAD v4: 17-60149936-G-C
MyVariant Identifiers: chr17:g.58227297G>C (hg19) chr17:g.60149936G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.60149936G>C , CM000679.2:g.60149936G>C GRCh38
NC_000017.10:g.58227297G>C , CM000679.1:g.58227297G>C GRCh37
NC_000017.9:g.55582079G>C NCBI36
NG_012050.1:g.4996G>C
NG_012050.2:g.4996G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300900.8:c.-99G>C ENSP00000300900.3:n.-99G>C
NM_000717.4:c.-99G>C NP_000708.1:n.-99G>C
NR_137422.1:n.1G>C
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