Canonical Allele Identifier: CA404896691

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18900090C>G (hg19) ; chr19:g.18789281C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18789281C>G , CM000681.2:g.18789281C>G	GRCh38
NC_000019.9:g.18900090C>G , CM000681.1:g.18900090C>G	GRCh37
NC_000019.8:g.18761090C>G	NCBI36
NG_007070.1:g.7025G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.407G>C MANE Select	ENSP00000222271.2:p.Cys136Ser
ENST00000222271.6:c.407G>C	ENSP00000222271.2:p.Cys136Ser
ENST00000425807.1:c.391-389G>C	ENSP00000403792.1:n.391-389G>C
ENST00000542601.6:c.308G>C	ENSP00000439156.2:p.Cys103Ser
NM_000095.2:c.407G>C	NP_000086.2:p.Cys136Ser
NM_000095.3:c.407G>C MANE Select	NP_000086.2:p.Cys136Ser