Canonical Allele Identifier: CA431116143
Gene: CRYGC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208994213T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129489T>C , CM000664.2:g.208129489T>C GRCh38
NC_000002.11:g.208994213T>C , CM000664.1:g.208994213T>C GRCh37
NC_000002.10:g.208702458T>C NCBI36
NG_008038.1:g.5342A>G
NG_008039.1:g.101A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.204A>G MANE Select ENSP00000282141.3:p.Gln68=
ENST00000282141.3:c.204A>G ENSP00000282141.3:p.Gln68=
NM_020989.3:c.204A>G NP_066269.1:p.Gln68=
NR_038437.1:n.98-7567T>C
XM_011510661.1:c.204A>G XP_011508963.1:p.Gln68=
XM_011510662.1:c.204A>G XP_011508964.1:p.Gln68=
XM_011510663.1:c.75A>G XP_011508965.1:p.Gln25=
NM_020989.4:c.204A>G MANE Select NP_066269.1:p.Gln68=
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