Canonical Allele Identifier: CA445402415
Gene: RASA1 HGNC NCBI

Linked Data

dbSNP Id: rs1580179548
MyVariant Identifiers: chr5:g.86564736T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268919T>G , CM000667.2:g.87268919T>G GRCh38
NC_000005.9:g.86564736T>G , CM000667.1:g.86564736T>G GRCh37
NC_000005.8:g.86600492T>G NCBI36
NG_011650.1:g.5586T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.468T>G MANE Select ENSP00000274376.6:p.Gly156=
ENST00000274376.10:c.468T>G ENSP00000274376.6:p.Gly156=
ENST00000515800.6:c.468T>G ENSP00000423395.2:p.Gly156=
NM_002890.2:c.468T>G NP_002881.1:p.Gly156=
XM_011543525.1:c.468T>G XP_011541827.1:p.Gly156=
XM_011543526.1:c.468T>G XP_011541828.1:p.Gly156=
XM_011543527.1:c.468T>G XP_011541829.1:p.Gly156=
XM_011543525.2:c.468T>G XP_011541827.1:p.Gly156=
XM_011543527.3:c.468T>G XP_011541829.1:p.Gly156=
NM_002890.3:c.468T>G MANE Select NP_002881.1:p.Gly156=