Canonical Allele Identifier: CA413942034

Gene: HNRNPH2 RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100667388C>T (hg19) ; chrX:g.101412400C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101412400C>T , CM000685.2:g.101412400C>T	GRCh38
NC_000023.10:g.100667388C>T , CM000685.1:g.100667388C>T	GRCh37
NC_000023.9:g.100554044C>T	NCBI36
NG_007119.1:g.564G>A , LRG_672:g.564G>A
NG_016327.1:g.9198C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316594.6:c.412C>T (HNRNPH2) MANE Select	ENSP00000361927.2:p.Pro138Ser
ENST00000316594.5:c.412C>T (HNRNPH2)	ENSP00000361927.2:p.Pro138Ser
NM_001032393.2:c.412C>T (HNRNPH2)	NP_001027565.1:p.Pro138Ser
NM_001199973.1:c.*408C>T (RPL36A-HNRNPH2)	NP_001186902.1:n.*408C>T
NM_001199974.1:c.*408C>T (RPL36A-HNRNPH2)	NP_001186903.1:n.*408C>T
NM_019597.4:c.412C>T (HNRNPH2)	NP_062543.1:p.Pro138Ser
NM_001199973.2:c.*408C>T (RPL36A-HNRNPH2)	NP_001186902.2:n.*408C>T
NM_001199974.2:c.*408C>T (RPL36A-HNRNPH2)	NP_001186903.2:n.*408C>T
NM_019597.5:c.412C>T (HNRNPH2) MANE Select	NP_062543.1:p.Pro138Ser
NM_001032393.3:c.412C>T (HNRNPH2)	NP_001027565.1:p.Pro138Ser