Canonical Allele Identifier: CA2259200451
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057246132
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665299A>G , CM000679.2:g.39665299A>G GRCh38
NC_000017.10:g.37821552A>G , CM000679.1:g.37821552A>G GRCh37
NC_000017.9:g.35075078A>G NCBI36
NG_008892.1:g.4954A>G , LRG_210:g.4954A>G
NG_042278.1:g.2319A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-61A>G ENSP00000312624.2:n.-61A>G
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