Canonical Allele Identifier: CA393097790

Gene: HCN4

Linked Data

• dbSNP Id: rs2043135658
• gnomAD v3: 15-73367760-G-A
• gnomAD v4: 15-73367760-G-A
• MyVariant Identifiers: chr15:g.73660101G>A (hg19) ; chr15:g.73367760G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367760G>A , CM000677.2:g.73367760G>A	GRCh38
NC_000015.9:g.73660101G>A , CM000677.1:g.73660101G>A	GRCh37
NC_000015.8:g.71447154G>A	NCBI36
NG_009063.1:g.6505C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.511C>T MANE Select	ENSP00000261917.3:p.Pro171Ser
ENST00000261917.3:c.511C>T	ENSP00000261917.3:p.Pro171Ser
NM_005477.2:c.511C>T	NP_005468.1:p.Pro171Ser
NM_005477.3:c.511C>T MANE Select	NP_005468.1:p.Pro171Ser