Canonical Allele Identifier: CA499889297
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs772083153
MyVariant Identifiers: chr17:g.37822260T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666007T>C , CM000679.2:g.39666007T>C GRCh38
NC_000017.10:g.37822260T>C , CM000679.1:g.37822260T>C GRCh37
NC_000017.9:g.35075786T>C NCBI36
NG_008892.1:g.5662T>C , LRG_210:g.5662T>C
NG_042278.1:g.3027T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.402T>C MANE Select ENSP00000312624.2:p.Ala134=
ENST00000309889.2:c.402T>C ENSP00000312624.2:p.Ala134=
ENST00000578283.1:c.330T>C ENSP00000462787.1:p.Ala110=
NM_003673.3:c.402T>C , LRG_210t1:c.402T>C NP_003664.1:p.Ala134=
NM_003673.4:c.402T>C MANE Select NP_003664.1:p.Ala134=
Search 100 bp 5'
Search 100 bp 3'