Canonical Allele Identifier: CA375219503

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308829C>T (hg19) ; chr9:g.130433442C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433442C>T , CM000671.2:g.130433442C>T	GRCh38
NC_000009.11:g.133308829C>T , CM000671.1:g.133308829C>T	GRCh37
NC_000009.10:g.132298650C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14932C>T	ENSP00000485357.2:p.His4978Tyr
ENST00000683500.2:c.14989C>T MANE Select	ENSP00000508292.2:p.His4997Tyr
ENST00000623487.1:n.3335C>T
ENST00000624552.3:c.14929C>T	ENSP00000485357.1:p.His4977Tyr
NM_001291815.1:c.14989C>T	NP_001278744.1:p.His4997Tyr
XM_011518465.1:c.14866C>T	XP_011516767.1:p.His4956Tyr
XM_011518466.1:c.14857C>T	XP_011516768.1:p.His4953Tyr
XM_011518467.1:c.14812C>T	XP_011516769.1:p.His4938Tyr
NM_001291815.2:c.14989C>T MANE Select	NP_001278744.1:p.His4997Tyr
XM_011518465.2:c.14866C>T	XP_011516767.1:p.His4956Tyr
XM_011518466.2:c.14857C>T	XP_011516768.1:p.His4953Tyr
XM_011518467.2:c.14812C>T	XP_011516769.1:p.His4938Tyr
XM_017014585.1:c.11770C>T	XP_016870074.1:p.His3924Tyr
XM_017014586.1:c.7567C>T	XP_016870075.1:p.His2523Tyr
XR_001746957.1:n.92+179G>A
XR_001746958.1:n.92+179G>A