Canonical Allele Identifier: CA343720028

Gene: MYOC

Linked Data

• MyVariant Identifiers: chr1:g.171621706G>T (hg19) ; chr1:g.171652566G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171652566G>T , CM000663.2:g.171652566G>T	GRCh38
NC_000001.10:g.171621706G>T , CM000663.1:g.171621706G>T	GRCh37
NC_000001.9:g.169888329G>T	NCBI36
NG_008859.1:g.5068C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000037502.11:c.46C>A MANE Select	ENSP00000037502.5:p.Pro16Thr
ENST00000638471.1:c.46C>A	ENSP00000491206.1:p.Pro16Thr
ENST00000037502.10:c.46C>A	ENSP00000037502.5:p.Pro16Thr
ENST00000614688.1:c.46C>A	ENSP00000478680.1:p.Pro16Thr
NM_000261.1:c.46C>A	NP_000252.1:p.Pro16Thr
NM_000261.2:c.46C>A MANE Select	NP_000252.1:p.Pro16Thr