Canonical Allele Identifier: CA2637631262
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39664858-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664858A>C , CM000679.2:g.39664858A>C GRCh38
NC_000017.10:g.37821111A>C , CM000679.1:g.37821111A>C GRCh37
NC_000017.9:g.35074637A>C NCBI36
NG_008892.1:g.4513A>C , LRG_210:g.4513A>C
NG_042278.1:g.1878A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-502A>C ENSP00000312624.2:n.-502A>C
Search 100 bp 5'
Search 100 bp 3'