Canonical Allele Identifier: CA359707740
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1244449353
gnomAD v2: 5-45645619-T-G
gnomAD v3: 5-45645517-T-G
gnomAD v4: 5-45645517-T-G
MyVariant Identifiers: chr5:g.45645619T>G (hg19) chr5:g.45645517T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645517T>G , CM000667.2:g.45645517T>G GRCh38
NC_000005.9:g.45645619T>G , CM000667.1:g.45645619T>G GRCh37
NC_000005.8:g.45681376T>G NCBI36
NG_042183.1:g.55602A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.517A>C MANE Select ENSP00000307342.4:p.Thr173Pro
ENST00000673735.1:c.517A>C ENSP00000501107.1:p.Thr173Pro
ENST00000303230.5:c.517A>C ENSP00000307342.4:p.Thr173Pro
ENST00000634658.1:c.517A>C ENSP00000489134.1:p.Thr173Pro
NM_021072.3:c.517A>C NP_066550.2:p.Thr173Pro
NM_021072.4:c.517A>C MANE Select NP_066550.2:p.Thr173Pro
Search 100 bp 5'
Search 100 bp 3'