Canonical Allele Identifier: CA559415947

Gene: HCN1

Linked Data

• dbSNP Id: rs1240580166
• gnomAD v2: 5-45461923-G-A
• gnomAD v4: 5-45461821-G-A
• MyVariant Identifiers: chr5:g.45461923G>A (hg19) ; chr5:g.45461821G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461821G>A , CM000667.2:g.45461821G>A	GRCh38
NC_000005.9:g.45461923G>A , CM000667.1:g.45461923G>A	GRCh37
NC_000005.8:g.45497680G>A	NCBI36
NG_042183.1:g.239298C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.1011+25C>T MANE Select	ENSP00000307342.4:n.1011+25C>T
ENST00000637305.1:n.174+25C>T
ENST00000673735.1:c.1011+25C>T	ENSP00000501107.1:n.1011+25C>T
ENST00000303230.5:c.1011+25C>T	ENSP00000307342.4:n.1011+25C>T
NM_021072.3:c.1011+25C>T	NP_066550.2:n.1011+25C>T
NM_021072.4:c.1011+25C>T MANE Select	NP_066550.2:n.1011+25C>T