Canonical Allele Identifier: CA491477903
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042870343
MyVariant Identifiers: chr15:g.73615221T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322880T>C , CM000677.2:g.73322880T>C GRCh38
NC_000015.9:g.73615221T>C , CM000677.1:g.73615221T>C GRCh37
NC_000015.8:g.71402274T>C NCBI36
NG_009063.1:g.51385A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3213A>G MANE Select ENSP00000261917.3:p.Thr1071=
ENST00000261917.3:c.3213A>G ENSP00000261917.3:p.Thr1071=
NM_005477.2:c.3213A>G NP_005468.1:p.Thr1071=
XM_011521148.1:c.1995A>G XP_011519450.1:p.Thr665=
XM_011521148.2:c.1995A>G XP_011519450.1:p.Thr665=
NM_005477.3:c.3213A>G MANE Select NP_005468.1:p.Thr1071=