Canonical Allele Identifier: CA499889173
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39665911-C-G
MyVariant Identifiers: chr17:g.37822164C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665911C>G , CM000679.2:g.39665911C>G GRCh38
NC_000017.10:g.37822164C>G , CM000679.1:g.37822164C>G GRCh37
NC_000017.9:g.35075690C>G NCBI36
NG_008892.1:g.5566C>G , LRG_210:g.5566C>G
NG_042278.1:g.2931C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.306C>G MANE Select ENSP00000312624.2:p.Thr102=
ENST00000309889.2:c.306C>G ENSP00000312624.2:p.Thr102=
ENST00000578283.1:c.234C>G ENSP00000462787.1:p.Thr78=
NM_003673.3:c.306C>G , LRG_210t1:c.306C>G NP_003664.1:p.Thr102=
NM_003673.4:c.306C>G MANE Select NP_003664.1:p.Thr102=
Search 100 bp 5'
Search 100 bp 3'