Canonical Allele Identifier: CA368219720
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404879A>T , CM000669.2:g.94404879A>T GRCh38
NC_000007.13:g.94034191A>T , CM000669.1:g.94034191A>T GRCh37
NC_000007.12:g.93872127A>T NCBI36
NG_007405.1:g.15319A>T , LRG_2:g.15319A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.419A>T MANE Select ENSP00000297268.6:p.Lys140Met
ENST00000297268.10:c.419A>T ENSP00000297268.6:p.Lys140Met
ENST00000620463.1:c.413A>T ENSP00000477719.1:p.Lys138Met
NM_000089.3:c.419A>T , LRG_2t1:c.419A>T NP_000080.2:p.Lys140Met
NM_000089.4:c.419A>T MANE Select NP_000080.2:p.Lys140Met