Canonical Allele Identifier: CA62589767
Gene: COL3A1 HGNC NCBI

Linked Data

dbSNP Id: rs536044672

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188989614A>T , CM000664.2:g.188989614A>T GRCh38
NC_000002.11:g.189854340A>T , CM000664.1:g.189854340A>T GRCh37
NC_000002.10:g.189562585A>T NCBI36
NG_007404.1:g.20242A>T , LRG_3:g.20242A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.690+165A>T ENSP00000415346.2:n.690+165A>T
ENST00000304636.9:c.690+165A>T MANE Select ENSP00000304408.4:n.690+165A>T
ENST00000304636.7:c.690+165A>T ENSP00000304408.3:n.690+165A>T
ENST00000317840.9:c.690+165A>T ENSP00000315243.6:n.690+165A>T
NM_000090.3:c.690+165A>T , LRG_3t1:c.690+165A>T NP_000081.1:n.690+165A>T
NM_000090.4:c.690+165A>T MANE Select NP_000081.2:n.690+165A>T