Canonical Allele Identifier: CA350097680
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129681G>C , CM000664.2:g.208129681G>C GRCh38
NC_000002.11:g.208994405G>C , CM000664.1:g.208994405G>C GRCh37
NC_000002.10:g.208702650G>C NCBI36
NG_008038.1:g.5150C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.12C>G MANE Select ENSP00000282141.3:p.Ile4Met
ENST00000282141.3:c.12C>G ENSP00000282141.3:p.Ile4Met
NM_020989.3:c.12C>G NP_066269.1:p.Ile4Met
NR_038437.1:n.98-7375G>C
XM_011510661.1:c.12C>G XP_011508963.1:p.Ile4Met
XM_011510662.1:c.12C>G XP_011508964.1:p.Ile4Met
XM_011510663.1:c.-118C>G XP_011508965.1:n.-118C>G
NM_020989.4:c.12C>G MANE Select NP_066269.1:p.Ile4Met