Canonical Allele Identifier: CA393090607

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73617365G>A (hg19) ; chr15:g.73325024G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73325024G>A , CM000677.2:g.73325024G>A	GRCh38
NC_000015.9:g.73617365G>A , CM000677.1:g.73617365G>A	GRCh37
NC_000015.8:g.71404418G>A	NCBI36
NG_009063.1:g.49241C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1909C>T MANE Select	ENSP00000261917.3:p.His637Tyr
ENST00000261917.3:c.1909C>T	ENSP00000261917.3:p.His637Tyr
NM_005477.2:c.1909C>T	NP_005468.1:p.His637Tyr
XM_011521148.1:c.691C>T	XP_011519450.1:p.His231Tyr
XM_011521148.2:c.691C>T	XP_011519450.1:p.His231Tyr
NM_005477.3:c.1909C>T MANE Select	NP_005468.1:p.His637Tyr