Canonical Allele Identifier: CA1323931497
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1695067664

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129688A>G , CM000664.2:g.208129688A>G GRCh38
NC_000002.11:g.208994412A>G , CM000664.1:g.208994412A>G GRCh37
NC_000002.10:g.208702657A>G NCBI36
NG_008038.1:g.5143T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-5T>C MANE Select ENSP00000282141.3:n.10-5T>C
ENST00000282141.3:c.10-5T>C ENSP00000282141.3:n.10-5T>C
NM_020989.3:c.10-5T>C NP_066269.1:n.10-5T>C
NR_038437.1:n.98-7368A>G
XM_011510661.1:c.10-5T>C XP_011508963.1:n.10-5T>C
XM_011510662.1:c.10-5T>C XP_011508964.1:n.10-5T>C
XM_011510663.1:c.-120-5T>C XP_011508965.1:n.-120-5T>C
NM_020989.4:c.10-5T>C MANE Select NP_066269.1:n.10-5T>C