Canonical Allele Identifier: CA2662869245
Gene: CRYGC HGNC NCBI

Linked Data

gnomAD v4: 2-208129687-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129687C>T , CM000664.2:g.208129687C>T GRCh38
NC_000002.11:g.208994411C>T , CM000664.1:g.208994411C>T GRCh37
NC_000002.10:g.208702656C>T NCBI36
NG_008038.1:g.5144G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-4G>A MANE Select ENSP00000282141.3:n.10-4G>A
ENST00000282141.3:c.10-4G>A ENSP00000282141.3:n.10-4G>A
NM_020989.3:c.10-4G>A NP_066269.1:n.10-4G>A
NR_038437.1:n.98-7369C>T
XM_011510661.1:c.10-4G>A XP_011508963.1:n.10-4G>A
XM_011510662.1:c.10-4G>A XP_011508964.1:n.10-4G>A
XM_011510663.1:c.-120-4G>A XP_011508965.1:n.-120-4G>A
NM_020989.4:c.10-4G>A MANE Select NP_066269.1:n.10-4G>A
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