Canonical Allele Identifier: CA340527445
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1417843189
gnomAD v2: 1-59042527-T-C
gnomAD v4: 1-58576855-T-C
MyVariant Identifiers: chr1:g.59042527T>C (hg19) chr1:g.58576855T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576855T>C , CM000663.2:g.58576855T>C GRCh38
NC_000001.10:g.59042527T>C , CM000663.1:g.59042527T>C GRCh37
NC_000001.9:g.58815115T>C NCBI36
NG_016237.1:g.5640A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.302A>G MANE Select ENSP00000360269.2:p.Asp101Gly
ENST00000371225.3:c.302A>G ENSP00000360269.2:p.Asp101Gly
NM_002353.2:c.302A>G NP_002344.2:p.Asp101Gly
NM_002353.3:c.302A>G MANE Select NP_002344.2:p.Asp101Gly
Search 100 bp 5'
Search 100 bp 3'