Canonical Allele Identifier: CA350096258
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129479G>T , CM000664.2:g.208129479G>T GRCh38
NC_000002.11:g.208994203G>T , CM000664.1:g.208994203G>T GRCh37
NC_000002.10:g.208702448G>T NCBI36
NG_008038.1:g.5352C>A
NG_008039.1:g.111C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.214C>A MANE Select ENSP00000282141.3:p.Leu72Ile
ENST00000282141.3:c.214C>A ENSP00000282141.3:p.Leu72Ile
NM_020989.3:c.214C>A NP_066269.1:p.Leu72Ile
NR_038437.1:n.98-7577G>T
XM_011510661.1:c.214C>A XP_011508963.1:p.Leu72Ile
XM_011510662.1:c.214C>A XP_011508964.1:p.Leu72Ile
XM_011510663.1:c.85C>A XP_011508965.1:p.Leu29Ile
NM_020989.4:c.214C>A MANE Select NP_066269.1:p.Leu72Ile