Canonical Allele Identifier: CA2637631271
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39664864-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664864C>T , CM000679.2:g.39664864C>T GRCh38
NC_000017.10:g.37821117C>T , CM000679.1:g.37821117C>T GRCh37
NC_000017.9:g.35074643C>T NCBI36
NG_008892.1:g.4519C>T , LRG_210:g.4519C>T
NG_042278.1:g.1884C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-496C>T ENSP00000312624.2:n.-496C>T
Search 100 bp 5'
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