Canonical Allele Identifier: CA762256618

Gene: COL5A2

Linked Data

• dbSNP Id: rs1277662611
• MyVariant Identifiers: chr2:g.189914984G>A (hg19) ; chr2:g.189050258G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189050258G>A , CM000664.2:g.189050258G>A	GRCh38
NC_000002.11:g.189914984G>A , CM000664.1:g.189914984G>A	GRCh37
NC_000002.10:g.189623229G>A	NCBI36
NG_011799.1:g.134622C>T
NG_011799.2:g.134622C>T
NG_011799.3:g.180044C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.3039+311C>T MANE Select	ENSP00000364000.3:n.3039+311C>T
ENST00000374866.7:c.3039+311C>T	ENSP00000364000.3:n.3039+311C>T
ENST00000618828.1:c.1878+311C>T	ENSP00000482184.1:n.1878+311C>T
NM_000393.3:c.3039+311C>T	NP_000384.2:n.3039+311C>T
XM_011510573.1:c.2901+311C>T	XP_011508875.1:n.2901+311C>T
NM_000393.4:c.3039+311C>T	NP_000384.2:n.3039+311C>T
XM_011510573.3:c.2901+311C>T	XP_011508875.1:n.2901+311C>T
NM_000393.5:c.3039+311C>T MANE Select	NP_000384.2:n.3039+311C>T