Canonical Allele Identifier: CA762208979
Gene: COL3A1 HGNC NCBI

Linked Data

dbSNP Id: rs1253683345

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189008617A>G , CM000664.2:g.189008617A>G GRCh38
NC_000002.11:g.189873343A>G , CM000664.1:g.189873343A>G GRCh37
NC_000002.10:g.189581588A>G NCBI36
NG_007404.1:g.39245A>G , LRG_3:g.39245A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.3427-307A>G ENSP00000415346.2:n.3427-307A>G
ENST00000304636.9:c.3526-307A>G MANE Select ENSP00000304408.4:n.3526-307A>G
ENST00000304636.7:c.3526-307A>G ENSP00000304408.3:n.3526-307A>G
ENST00000317840.9:c.2617-307A>G ENSP00000315243.6:n.2617-307A>G
ENST00000487010.1:n.316A>G
NM_000090.3:c.3526-307A>G , LRG_3t1:c.3526-307A>G NP_000081.1:n.3526-307A>G
NM_000090.4:c.3526-307A>G MANE Select NP_000081.2:n.3526-307A>G