Canonical Allele Identifier: CA402887178

Gene: HCN2

Linked Data

• gnomAD v4: 19-616011-T-G
• MyVariant Identifiers: chr19:g.616011T>G (hg19) ; chr19:g.616011T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.616011T>G , CM000681.2:g.616011T>G	GRCh38
NC_000019.9:g.616011T>G , CM000681.1:g.616011T>G	GRCh37
NC_000019.8:g.567011T>G	NCBI36
NG_023049.1:g.22558A>C
NG_052810.1:g.31119T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251287.3:c.2207T>G MANE Select	ENSP00000251287.1:p.Met736Arg
ENST00000251287.2:c.2207T>G	ENSP00000251287.1:p.Met736Arg
NM_001194.3:c.2207T>G	NP_001185.3:p.Met736Arg
NM_001194.4:c.2207T>G MANE Select	NP_001185.3:p.Met736Arg