Canonical Allele Identifier: CA431116199
Gene: CRYGC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208994258A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129534A>C , CM000664.2:g.208129534A>C GRCh38
NC_000002.11:g.208994258A>C , CM000664.1:g.208994258A>C GRCh37
NC_000002.10:g.208702503A>C NCBI36
NG_008038.1:g.5297T>G
NG_008039.1:g.56T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.159T>G MANE Select ENSP00000282141.3:p.Gly53=
ENST00000282141.3:c.159T>G ENSP00000282141.3:p.Gly53=
NM_020989.3:c.159T>G NP_066269.1:p.Gly53=
NR_038437.1:n.98-7522A>C
XM_011510661.1:c.159T>G XP_011508963.1:p.Gly53=
XM_011510662.1:c.159T>G XP_011508964.1:p.Gly53=
XM_011510663.1:c.30T>G XP_011508965.1:p.Gly10=
NM_020989.4:c.159T>G MANE Select NP_066269.1:p.Gly53=
Search 100 bp 5'
Search 100 bp 3'