Canonical Allele Identifier: CA1881266262
Gene: HMCN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130433404A= , CM000671.2:g.130433404A= GRCh38
NC_000009.11:g.133308791A= , CM000671.1:g.133308791A= GRCh37
NC_000009.10:g.132298612A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14894A= ENSP00000485357.2:p.Gln4965=
ENST00000683500.2:c.14951A= MANE Select ENSP00000508292.2:p.Gln4984=
ENST00000623487.1:n.3297A=
ENST00000624552.3:c.14891A= ENSP00000485357.1:p.Gln4964=
NM_001291815.1:c.14951A= NP_001278744.1:p.Gln4984=
XM_011518465.1:c.14828A= XP_011516767.1:p.Gln4943=
XM_011518466.1:c.14819A= XP_011516768.1:p.Gln4940=
XM_011518467.1:c.14774A= XP_011516769.1:p.Gln4925=
NM_001291815.2:c.14951A= MANE Select NP_001278744.1:p.Gln4984=
XM_011518465.2:c.14828A= XP_011516767.1:p.Gln4943=
XM_011518466.2:c.14819A= XP_011516768.1:p.Gln4940=
XM_011518467.2:c.14774A= XP_011516769.1:p.Gln4925=
XM_017014585.1:c.11732A= XP_016870074.1:p.Gln3911=
XM_017014586.1:c.7529A= XP_016870075.1:p.Gln2510=
XR_001746957.1:n.92+217T=
XR_001746958.1:n.92+217T=