Canonical Allele Identifier: CA499670549
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145074864
MyVariant Identifiers: chr17:g.37822317T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666064T>C , CM000679.2:g.39666064T>C GRCh38
NC_000017.10:g.37822317T>C , CM000679.1:g.37822317T>C GRCh37
NC_000017.9:g.35075843T>C NCBI36
NG_008892.1:g.5719T>C , LRG_210:g.5719T>C
NG_042278.1:g.3084T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.459T>C MANE Select ENSP00000312624.2:p.Arg153=
ENST00000309889.2:c.459T>C ENSP00000312624.2:p.Arg153=
ENST00000578283.1:c.387T>C ENSP00000462787.1:p.Arg129=
NM_003673.3:c.459T>C , LRG_210t1:c.459T>C NP_003664.1:p.Arg153=
NM_003673.4:c.459T>C MANE Select NP_003664.1:p.Arg153=
Search 100 bp 5'
Search 100 bp 3'