Canonical Allele Identifier: CA492076277
Gene: RLBP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.89755067G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211836G>C , CM000677.2:g.89211836G>C GRCh38
NC_000015.9:g.89755067G>C , CM000677.1:g.89755067G>C GRCh37
NC_000015.8:g.87556071G>C NCBI36
NG_008116.1:g.14856C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268125.10:c.591C>G MANE Select ENSP00000268125.5:p.Gly197=
ENST00000268125.9:c.591C>G ENSP00000268125.5:p.Gly197=
ENST00000563254.1:c.8C>G
ENST00000567787.1:c.*169C>G ENSP00000457251.1:n.*169C>G
NM_000326.4:c.591C>G NP_000317.1:p.Gly197=
XM_011521870.1:c.591C>G XP_011520172.1:p.Gly197=
XM_011521871.1:c.516C>G XP_011520173.1:p.Gly172=
XM_011521872.1:c.516C>G XP_011520174.1:p.Gly172=
XM_011521870.2:c.591C>G XP_011520172.1:p.Gly197=
XM_017022460.1:c.618C>G XP_016877949.1:p.Gly206=
NM_000326.5:c.591C>G MANE Select NP_000317.1:p.Gly197=