Canonical Allele Identifier: CA1543790569
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645398C= , CM000667.2:g.45645398C= GRCh38
NC_000005.9:g.45645500C= , CM000667.1:g.45645500C= GRCh37
NC_000005.8:g.45681257C= NCBI36
NG_042183.1:g.55721G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.636G= MANE Select ENSP00000307342.4:p.Val212=
ENST00000673735.1:c.636G= ENSP00000501107.1:p.Val212=
ENST00000303230.5:c.636G= ENSP00000307342.4:p.Val212=
ENST00000634658.1:c.636G= ENSP00000489134.1:p.Val212=
NM_021072.3:c.636G= NP_066550.2:p.Val212=
NM_021072.4:c.636G= MANE Select NP_066550.2:p.Val212=