Canonical Allele Identifier: CA359707952
Gene: HCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.45645710C>G (hg19) chr5:g.45645608C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645608C>G , CM000667.2:g.45645608C>G GRCh38
NC_000005.9:g.45645710C>G , CM000667.1:g.45645710C>G GRCh37
NC_000005.8:g.45681467C>G NCBI36
NG_042183.1:g.55511G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.426G>C MANE Select ENSP00000307342.4:p.Arg142Ser
ENST00000673735.1:c.426G>C ENSP00000501107.1:p.Arg142Ser
ENST00000303230.5:c.426G>C ENSP00000307342.4:p.Arg142Ser
ENST00000634658.1:c.426G>C ENSP00000489134.1:p.Arg142Ser
NM_021072.3:c.426G>C NP_066550.2:p.Arg142Ser
NM_021072.4:c.426G>C MANE Select NP_066550.2:p.Arg142Ser
Search 100 bp 5'
Search 100 bp 3'