Canonical Allele Identifier: CA1726781661
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94425660C= , CM000669.2:g.94425660C= GRCh38
NC_000007.13:g.94054972C= , CM000669.1:g.94054972C= GRCh37
NC_000007.12:g.93892908C= NCBI36
NG_007405.1:g.36100C= , LRG_2:g.36100C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2832C= MANE Select ENSP00000297268.6:p.His944=
ENST00000297268.10:c.2832C= ENSP00000297268.6:p.His944=
ENST00000469732.1:n.615C=
ENST00000478215.1:n.391C=
ENST00000481570.5:n.2805C=
ENST00000620463.1:c.2826C= ENSP00000477719.1:p.His942=
NM_000089.3:c.2832C= , LRG_2t1:c.2832C= NP_000080.2:p.His944=
NM_000089.4:c.2832C= MANE Select NP_000080.2:p.His944=