Canonical Allele Identifier: CA393097790
Gene: HCN4 HGNC NCBI

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)
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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
Search 100 bp 5'
Search 100 bp 3'