Canonical Allele Identifier: CA2637631329
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39664923-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664923A>C , CM000679.2:g.39664923A>C GRCh38
NC_000017.10:g.37821176A>C , CM000679.1:g.37821176A>C GRCh37
NC_000017.9:g.35074702A>C NCBI36
NG_008892.1:g.4578A>C , LRG_210:g.4578A>C
NG_042278.1:g.1943A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-437A>C ENSP00000312624.2:n.-437A>C
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