Canonical Allele Identifier: CA11155342
Gene: TACR1 HGNC NCBI

Linked Data

dbSNP Id: rs6741029
gnomAD v2: 2-75345195-T-G
gnomAD v3: 2-75118069-T-G
gnomAD v4: 2-75118069-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.75118069T>G , CM000664.2:g.75118069T>G GRCh38
NC_000002.11:g.75345195T>G , CM000664.1:g.75345195T>G GRCh37
NC_000002.10:g.75198703T>G NCBI36
NG_029522.1:g.86451A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305249.10:c.584+2505A>C MANE Select ENSP00000303522.4:n.584+2505A>C
ENST00000305249.9:c.584+2505A>C ENSP00000303522.4:n.584+2505A>C
ENST00000409848.3:c.584+2505A>C ENSP00000386448.3:n.584+2505A>C
NM_001058.3:c.584+2505A>C NP_001049.1:n.584+2505A>C
NM_015727.2:c.584+2505A>C NP_056542.1:n.584+2505A>C
NM_001058.4:c.584+2505A>C MANE Select NP_001049.1:n.584+2505A>C
NM_015727.3:c.584+2505A>C NP_056542.1:n.584+2505A>C