Canonical Allele Identifier: CA272663993
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs988840779
gnomAD v2: 15-73615462-A-G
gnomAD v4: 15-73323121-A-G
MyVariant Identifiers: chr15:g.73615462A>G (hg19) chr15:g.73323121A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323121A>G , CM000677.2:g.73323121A>G GRCh38
NC_000015.9:g.73615462A>G , CM000677.1:g.73615462A>G GRCh37
NC_000015.8:g.71402515A>G NCBI36
NG_009063.1:g.51144T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2972T>C MANE Select ENSP00000261917.3:p.Leu991Pro
ENST00000261917.3:c.2972T>C ENSP00000261917.3:p.Leu991Pro
NM_005477.2:c.2972T>C NP_005468.1:p.Leu991Pro
XM_011521148.1:c.1754T>C XP_011519450.1:p.Leu585Pro
XM_011521148.2:c.1754T>C XP_011519450.1:p.Leu585Pro
NM_005477.3:c.2972T>C MANE Select NP_005468.1:p.Leu991Pro
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