Canonical Allele Identifier: CA1881266242
Gene: HMCN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130433395C= , CM000671.2:g.130433395C= GRCh38
NC_000009.11:g.133308782C= , CM000671.1:g.133308782C= GRCh37
NC_000009.10:g.132298603C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624552.4:c.14885C= ENSP00000485357.2:p.Ser4962=
ENST00000683500.2:c.14942C= MANE Select ENSP00000508292.2:p.Ser4981=
ENST00000623487.1:n.3288C=
ENST00000624552.3:c.14882C= ENSP00000485357.1:p.Ser4961=
NM_001291815.1:c.14942C= NP_001278744.1:p.Ser4981=
XM_011518465.1:c.14819C= XP_011516767.1:p.Ser4940=
XM_011518466.1:c.14810C= XP_011516768.1:p.Ser4937=
XM_011518467.1:c.14765C= XP_011516769.1:p.Ser4922=
NM_001291815.2:c.14942C= MANE Select NP_001278744.1:p.Ser4981=
XM_011518465.2:c.14819C= XP_011516767.1:p.Ser4940=
XM_011518466.2:c.14810C= XP_011516768.1:p.Ser4937=
XM_011518467.2:c.14765C= XP_011516769.1:p.Ser4922=
XM_017014585.1:c.11723C= XP_016870074.1:p.Ser3908=
XM_017014586.1:c.7520C= XP_016870075.1:p.Ser2507=
XR_001746957.1:n.92+226G=
XR_001746958.1:n.92+226G=