Canonical Allele Identifier: CA421938468

Linked Data

MyVariant Identifiers: chr1:g.171605383A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636243A>T , CM000663.2:g.171636243A>T GRCh38
NC_000001.10:g.171605383A>T , CM000663.1:g.171605383A>T GRCh37
NC_000001.9:g.169872006A>T NCBI36
NG_008859.1:g.21391T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1197T>A (MYOC) MANE Select ENSP00000037502.5:p.Gly399=
ENST00000637303.1:c.235-2387A>T (MYOCOS) ENSP00000490048.1:n.235-2387A>T
ENST00000638471.1:c.*535T>A (MYOC) ENSP00000491206.1:n.*535T>A
ENST00000037502.10:c.1197T>A (MYOC) ENSP00000037502.5:p.Gly399=
ENST00000614688.1:c.*161T>A (MYOC) ENSP00000478680.1:n.*161T>A
NM_000261.1:c.1197T>A (MYOC) NP_000252.1:p.Gly399=
NM_000261.2:c.1197T>A (MYOC) MANE Select NP_000252.1:p.Gly399=