Canonical Allele Identifier: CA2776991462
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409305T>C , CM000669.2:g.94409305T>C GRCh38
NC_000007.13:g.94038617T>C , CM000669.1:g.94038617T>C GRCh37
NC_000007.12:g.93876553T>C NCBI36
NG_007405.1:g.19745T>C , LRG_2:g.19745T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.793-17T>C MANE Select ENSP00000297268.6:n.793-17T>C
ENST00000297268.10:c.793-17T>C ENSP00000297268.6:n.793-17T>C
ENST00000620463.1:c.787-17T>C ENSP00000477719.1:n.787-17T>C
NM_000089.3:c.793-17T>C , LRG_2t1:c.793-17T>C NP_000080.2:n.793-17T>C
NM_000089.4:c.793-17T>C MANE Select NP_000080.2:n.793-17T>C