Canonical Allele Identifier: CA375219356

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308792G>C (hg19) ; chr9:g.130433405G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433405G>C , CM000671.2:g.130433405G>C	GRCh38
NC_000009.11:g.133308792G>C , CM000671.1:g.133308792G>C	GRCh37
NC_000009.10:g.132298613G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14895G>C	ENSP00000485357.2:p.Gln4965His
ENST00000683500.2:c.14952G>C MANE Select	ENSP00000508292.2:p.Gln4984His
ENST00000623487.1:n.3298G>C
ENST00000624552.3:c.14892G>C	ENSP00000485357.1:p.Gln4964His
NM_001291815.1:c.14952G>C	NP_001278744.1:p.Gln4984His
XM_011518465.1:c.14829G>C	XP_011516767.1:p.Gln4943His
XM_011518466.1:c.14820G>C	XP_011516768.1:p.Gln4940His
XM_011518467.1:c.14775G>C	XP_011516769.1:p.Gln4925His
NM_001291815.2:c.14952G>C MANE Select	NP_001278744.1:p.Gln4984His
XM_011518465.2:c.14829G>C	XP_011516767.1:p.Gln4943His
XM_011518466.2:c.14820G>C	XP_011516768.1:p.Gln4940His
XM_011518467.2:c.14775G>C	XP_011516769.1:p.Gln4925His
XM_017014585.1:c.11733G>C	XP_016870074.1:p.Gln3911His
XM_017014586.1:c.7530G>C	XP_016870075.1:p.Gln2510His
XR_001746957.1:n.92+216C>G
XR_001746958.1:n.92+216C>G