Canonical Allele Identifier: CA1323931507
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1695068349

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129708T>A , CM000664.2:g.208129708T>A GRCh38
NC_000002.11:g.208994432T>A , CM000664.1:g.208994432T>A GRCh37
NC_000002.10:g.208702677T>A NCBI36
NG_008038.1:g.5123A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-25A>T MANE Select ENSP00000282141.3:n.10-25A>T
ENST00000282141.3:c.10-25A>T ENSP00000282141.3:n.10-25A>T
NM_020989.3:c.10-25A>T NP_066269.1:n.10-25A>T
NR_038437.1:n.98-7348T>A
XM_011510661.1:c.10-25A>T XP_011508963.1:n.10-25A>T
XM_011510662.1:c.10-25A>T XP_011508964.1:n.10-25A>T
XM_011510663.1:c.-120-25A>T XP_011508965.1:n.-120-25A>T
NM_020989.4:c.10-25A>T MANE Select NP_066269.1:n.10-25A>T