Canonical Allele Identifier: CA1726781668
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94425662A= , CM000669.2:g.94425662A= GRCh38
NC_000007.13:g.94054974A= , CM000669.1:g.94054974A= GRCh37
NC_000007.12:g.93892910A= NCBI36
NG_007405.1:g.36102A= , LRG_2:g.36102A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2834A= MANE Select ENSP00000297268.6:p.Lys945=
ENST00000297268.10:c.2834A= ENSP00000297268.6:p.Lys945=
ENST00000469732.1:n.617A=
ENST00000478215.1:n.393A=
ENST00000481570.5:n.2807A=
ENST00000620463.1:c.2828A= ENSP00000477719.1:p.Lys943=
NM_000089.3:c.2834A= , LRG_2t1:c.2834A= NP_000080.2:p.Lys945=
NM_000089.4:c.2834A= MANE Select NP_000080.2:p.Lys945=