Canonical Allele Identifier: CA430307739
Gene: COL5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189963483T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189098757T>C , CM000664.2:g.189098757T>C GRCh38
NC_000002.11:g.189963483T>C , CM000664.1:g.189963483T>C GRCh37
NC_000002.10:g.189671728T>C NCBI36
NG_011799.1:g.86123A>G
NG_011799.2:g.86123A>G
NG_011799.3:g.131545A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374866.9:c.372A>G MANE Select ENSP00000364000.3:p.Val124=
ENST00000649966.1:c.234A>G ENSP00000496785.1:p.Val78=
ENST00000374866.7:c.372A>G ENSP00000364000.3:p.Val124=
ENST00000618828.1:c.-259A>G ENSP00000482184.1:n.-259A>G
NM_000393.3:c.372A>G NP_000384.2:p.Val124=
XM_011510573.1:c.234A>G XP_011508875.1:p.Val78=
NM_000393.4:c.372A>G NP_000384.2:p.Val124=
XM_011510573.3:c.234A>G XP_011508875.1:p.Val78=
NM_000393.5:c.372A>G MANE Select NP_000384.2:p.Val124=