Canonical Allele Identifier: CA375219283

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308775G>C (hg19) ; chr9:g.130433388G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433388G>C , CM000671.2:g.130433388G>C	GRCh38
NC_000009.11:g.133308775G>C , CM000671.1:g.133308775G>C	GRCh37
NC_000009.10:g.132298596G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14878G>C	ENSP00000485357.2:p.Gly4960Arg
ENST00000683500.2:c.14935G>C MANE Select	ENSP00000508292.2:p.Gly4979Arg
ENST00000623487.1:n.3281G>C
ENST00000624552.3:c.14875G>C	ENSP00000485357.1:p.Gly4959Arg
NM_001291815.1:c.14935G>C	NP_001278744.1:p.Gly4979Arg
XM_011518465.1:c.14812G>C	XP_011516767.1:p.Gly4938Arg
XM_011518466.1:c.14803G>C	XP_011516768.1:p.Gly4935Arg
XM_011518467.1:c.14758G>C	XP_011516769.1:p.Gly4920Arg
NM_001291815.2:c.14935G>C MANE Select	NP_001278744.1:p.Gly4979Arg
XM_011518465.2:c.14812G>C	XP_011516767.1:p.Gly4938Arg
XM_011518466.2:c.14803G>C	XP_011516768.1:p.Gly4935Arg
XM_011518467.2:c.14758G>C	XP_011516769.1:p.Gly4920Arg
XM_017014585.1:c.11716G>C	XP_016870074.1:p.Gly3906Arg
XM_017014586.1:c.7513G>C	XP_016870075.1:p.Gly2505Arg
XR_001746957.1:n.92+233C>G
XR_001746958.1:n.92+233C>G