Canonical Allele Identifier: CA1209753599
Gene: RASAL2 HGNC NCBI

Linked Data

dbSNP Id: rs316274

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.178173073G>C , CM000663.2:g.178173073G>C GRCh38
NC_000001.10:g.178142208G>C , CM000663.1:g.178142208G>C GRCh37
NC_000001.9:g.176408831G>C NCBI36
NG_047109.1:g.84345G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367649.8:c.202+78379G>C MANE Select ENSP00000356621.3:n.202+78379G>C
ENST00000367649.7:c.202+78379G>C ENSP00000356621.3:n.202+78379G>C
ENST00000465723.1:n.526+47572G>C
NM_170692.2:c.202+78379G>C NP_733793.2:n.202+78379G>C
XM_011510166.1:c.202+78379G>C XP_011508468.1:n.202+78379G>C
XM_011510167.1:c.202+78379G>C XP_011508469.1:n.202+78379G>C
XM_011510168.1:c.202+78379G>C XP_011508470.1:n.202+78379G>C
XM_011510166.2:c.202+78379G>C XP_011508468.1:n.202+78379G>C
XM_011510167.2:c.202+78379G>C XP_011508469.1:n.202+78379G>C
NM_170692.4:c.202+78379G>C MANE Select NP_733793.2:n.202+78379G>C