Canonical Allele Identifier: CA359704607

Gene: HCN1

Linked Data

• MyVariant Identifiers: chr5:g.45461946A>G (hg19) ; chr5:g.45461844A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461844A>G , CM000667.2:g.45461844A>G	GRCh38
NC_000005.9:g.45461946A>G , CM000667.1:g.45461946A>G	GRCh37
NC_000005.8:g.45497703A>G	NCBI36
NG_042183.1:g.239275T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000303230.6:c.1011+2T>C MANE Select	ENSP00000307342.4:n.1011+2T>C
ENST00000637305.1:n.174+2T>C
ENST00000673735.1:c.1011+2T>C	ENSP00000501107.1:n.1011+2T>C
ENST00000303230.5:c.1011+2T>C	ENSP00000307342.4:n.1011+2T>C
NM_021072.3:c.1011+2T>C	NP_066550.2:n.1011+2T>C
NM_021072.4:c.1011+2T>C MANE Select	NP_066550.2:n.1011+2T>C