Canonical Allele Identifier: CA118324601

Gene: HCN1

Linked Data

• dbSNP Id: rs768413675
• MyVariant Identifiers: chr5:g.45645233C>A (hg19) ; chr5:g.45645131C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645131C>A , CM000667.2:g.45645131C>A	GRCh38
NC_000005.9:g.45645233C>A , CM000667.1:g.45645233C>A	GRCh37
NC_000005.8:g.45680990C>A	NCBI36
NG_042183.1:g.55988G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000303230.6:c.849+54G>T MANE Select	ENSP00000307342.4:n.849+54G>T
ENST00000637256.1:n.77+54G>T
ENST00000673735.1:c.849+54G>T	ENSP00000501107.1:n.849+54G>T
ENST00000303230.5:c.849+54G>T	ENSP00000307342.4:n.849+54G>T
ENST00000634658.1:c.*15G>T	ENSP00000489134.1:n.*15G>T
NM_021072.3:c.849+54G>T	NP_066550.2:n.849+54G>T
NM_021072.4:c.849+54G>T MANE Select	NP_066550.2:n.849+54G>T