Canonical Allele Identifier: CA074732
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 333057
dbSNP Id: rs373838193

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188997376C>T , CM000664.2:g.188997376C>T GRCh38
NC_000002.11:g.189862102C>T , CM000664.1:g.189862102C>T GRCh37
NC_000002.10:g.189570347C>T NCBI36
NG_007404.1:g.28004C>T , LRG_3:g.28004C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.1757C>T ENSP00000415346.2:p.Pro586Leu
ENST00000304636.9:c.1856C>T MANE Select ENSP00000304408.4:p.Pro619Leu
ENST00000304636.7:c.1856C>T ENSP00000304408.3:p.Pro619Leu
ENST00000317840.9:c.1856C>T ENSP00000315243.6:p.Pro619Leu
NM_000090.3:c.1856C>T , LRG_3t1:c.1856C>T NP_000081.1:p.Pro619Leu
NM_000090.4:c.1856C>T MANE Select NP_000081.2:p.Pro619Leu