Canonical Allele Identifier: CA290433656
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs77831798
MyVariant Identifiers: chr17:g.37821601T>A (hg19) chr17:g.39665348T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665348T>A , CM000679.2:g.39665348T>A GRCh38
NC_000017.10:g.37821601T>A , CM000679.1:g.37821601T>A GRCh37
NC_000017.9:g.35075127T>A NCBI36
NG_008892.1:g.5003T>A , LRG_210:g.5003T>A
NG_042278.1:g.2368T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-12T>A ENSP00000312624.2:n.-12T>A
NM_003673.3:c.-12T>A , LRG_210t1:c.-12T>A NP_003664.1:n.-12T>A
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