Canonical Allele Identifier: CA1726790790
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401362G= , CM000669.2:g.94401362G= GRCh38
NC_000007.13:g.94030674G= , CM000669.1:g.94030674G= GRCh37
NC_000007.12:g.93868610G= NCBI36
NG_007405.1:g.11802G= , LRG_2:g.11802G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-205G= MANE Select ENSP00000297268.6:n.226-205G=
ENST00000297268.10:c.226-205G= ENSP00000297268.6:n.226-205G=
ENST00000620463.1:c.220-205G= ENSP00000477719.1:n.220-205G=
NM_000089.3:c.226-205G= , LRG_2t1:c.226-205G= NP_000080.2:n.226-205G=
NM_000089.4:c.226-205G= MANE Select NP_000080.2:n.226-205G=