Canonical Allele Identifier: CA1726792169
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404618G= , CM000669.2:g.94404618G= GRCh38
NC_000007.13:g.94033930G= , CM000669.1:g.94033930G= GRCh37
NC_000007.12:g.93871866G= NCBI36
NG_007405.1:g.15058G= , LRG_2:g.15058G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.324+18G= MANE Select ENSP00000297268.6:n.324+18G=
ENST00000297268.10:c.324+18G= ENSP00000297268.6:n.324+18G=
ENST00000620463.1:c.318+18G= ENSP00000477719.1:n.318+18G=
NM_000089.3:c.324+18G= , LRG_2t1:c.324+18G= NP_000080.2:n.324+18G=
NM_000089.4:c.324+18G= MANE Select NP_000080.2:n.324+18G=