Canonical Allele Identifier: CA877433
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs532383713
gnomAD v2: 1-59042417-T-C
gnomAD v3: 1-58576745-T-C
gnomAD v4: 1-58576745-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576745T>C , CM000663.2:g.58576745T>C GRCh38
NC_000001.10:g.59042417T>C , CM000663.1:g.59042417T>C GRCh37
NC_000001.9:g.58815005T>C NCBI36
NG_016237.1:g.5750A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.412A>G MANE Select ENSP00000360269.2:p.Lys138Glu
ENST00000371225.3:c.412A>G ENSP00000360269.2:p.Lys138Glu
NM_002353.2:c.412A>G NP_002344.2:p.Lys138Glu
NM_002353.3:c.412A>G MANE Select NP_002344.2:p.Lys138Glu