Canonical Allele Identifier: CA29083804
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs560494997
gnomAD v3: 1-115033788-G-C
gnomAD v4: 1-115033788-G-C
MyVariant Identifiers: chr1:g.115576409G>C (hg19) chr1:g.115033788G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033788G>C , CM000663.2:g.115033788G>C GRCh38
NC_000001.10:g.115576409G>C , CM000663.1:g.115576409G>C GRCh37
NC_000001.9:g.115377932G>C NCBI36
NG_015891.1:g.8995G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-185G>C MANE Select ENSP00000256592.1:n.163-185G>C
ENST00000256592.2:c.163-185G>C ENSP00000256592.1:n.163-185G>C
ENST00000369517.1:c.163-185G>C ENSP00000358530.1:n.163-185G>C
NM_000549.4:c.163-185G>C NP_000540.2:n.163-185G>C
XM_011542065.1:c.163-185G>C XP_011540367.1:n.163-185G>C
XM_011542065.2:c.163-185G>C XP_011540367.1:n.163-185G>C
NM_000549.5:c.163-185G>C MANE Select NP_000540.2:n.163-185G>C
Search 100 bp 5'
Search 100 bp 3'