Canonical Allele Identifier: CA11101795
Gene: NGEF HGNC NCBI

Linked Data

dbSNP Id: rs11678490

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232966240G>A , CM000664.2:g.232966240G>A GRCh38
NC_000002.11:g.233830950G>A , CM000664.1:g.233830950G>A GRCh37
NC_000002.10:g.233539194G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264051.8:c.383+3974C>T MANE Select ENSP00000264051.3:n.383+3974C>T
ENST00000264051.7:c.383+3974C>T ENSP00000264051.3:n.383+3974C>T
NM_019850.2:c.383+3974C>T NP_062824.2:n.383+3974C>T
XM_011510923.1:c.383+3974C>T XP_011509225.1:n.383+3974C>T
XM_011510923.3:c.383+3974C>T XP_011509225.1:n.383+3974C>T
NM_019850.3:c.383+3974C>T MANE Select NP_062824.2:n.383+3974C>T