Canonical Allele Identifier: CA2683769661
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94415167-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415167C>T , CM000669.2:g.94415167C>T GRCh38
NC_000007.13:g.94044479C>T , CM000669.1:g.94044479C>T GRCh37
NC_000007.12:g.93882415C>T NCBI36
NG_007405.1:g.25607C>T , LRG_2:g.25607C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1720-59C>T MANE Select ENSP00000297268.6:n.1720-59C>T
ENST00000297268.10:c.1720-59C>T ENSP00000297268.6:n.1720-59C>T
ENST00000473573.5:n.57-59C>T
ENST00000488298.5:n.144-59C>T
ENST00000620463.1:c.1714-59C>T ENSP00000477719.1:n.1714-59C>T
NM_000089.3:c.1720-59C>T , LRG_2t1:c.1720-59C>T NP_000080.2:n.1720-59C>T
NM_000089.4:c.1720-59C>T MANE Select NP_000080.2:n.1720-59C>T