Canonical Allele Identifier: CA290433302
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs535319258
gnomAD v2: 17-37821193-G-C
gnomAD v3: 17-39664940-G-C
gnomAD v4: 17-39664940-G-C
MyVariant Identifiers: chr17:g.37821193G>C (hg19) chr17:g.39664940G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664940G>C , CM000679.2:g.39664940G>C GRCh38
NC_000017.10:g.37821193G>C , CM000679.1:g.37821193G>C GRCh37
NC_000017.9:g.35074719G>C NCBI36
NG_008892.1:g.4595G>C , LRG_210:g.4595G>C
NG_042278.1:g.1960G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-420G>C ENSP00000312624.2:n.-420G>C
Search 100 bp 5'
Search 100 bp 3'