Canonical Allele Identifier: CA32685642

Gene: MYOC MYOCOS

Linked Data

• dbSNP Id: rs1056051290
• MyVariant Identifiers: chr1:g.171605369G>T (hg19) ; chr1:g.171636229G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171636229G>T , CM000663.2:g.171636229G>T	GRCh38
NC_000001.10:g.171605369G>T , CM000663.1:g.171605369G>T	GRCh37
NC_000001.9:g.169871992G>T	NCBI36
NG_008859.1:g.21405C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000037502.11:c.1211C>A (MYOC) MANE Select	ENSP00000037502.5:p.Ser404Tyr
ENST00000637303.1:c.235-2401G>T (MYOCOS)	ENSP00000490048.1:n.235-2401G>T
ENST00000638471.1:c.*549C>A (MYOC)	ENSP00000491206.1:n.*549C>A
ENST00000037502.10:c.1211C>A (MYOC)	ENSP00000037502.5:p.Ser404Tyr
ENST00000614688.1:c.*175C>A (MYOC)	ENSP00000478680.1:n.*175C>A
NM_000261.1:c.1211C>A (MYOC)	NP_000252.1:p.Ser404Tyr
NM_000261.2:c.1211C>A (MYOC) MANE Select	NP_000252.1:p.Ser404Tyr