Canonical Allele Identifier: CA2637631380
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39664969-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664969G>A , CM000679.2:g.39664969G>A GRCh38
NC_000017.10:g.37821222G>A , CM000679.1:g.37821222G>A GRCh37
NC_000017.9:g.35074748G>A NCBI36
NG_008892.1:g.4624G>A , LRG_210:g.4624G>A
NG_042278.1:g.1989G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-391G>A ENSP00000312624.2:n.-391G>A
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