Canonical Allele Identifier: CA492076010
Gene: RLBP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.89755013G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211782G>C , CM000677.2:g.89211782G>C GRCh38
NC_000015.9:g.89755013G>C , CM000677.1:g.89755013G>C GRCh37
NC_000015.8:g.87556017G>C NCBI36
NG_008116.1:g.14910C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000268125.10:c.645C>G MANE Select ENSP00000268125.5:p.Leu215=
ENST00000268125.9:c.645C>G ENSP00000268125.5:p.Leu215=
ENST00000563254.1:c.62C>G
ENST00000567787.1:c.*223C>G ENSP00000457251.1:n.*223C>G
NM_000326.4:c.645C>G NP_000317.1:p.Leu215=
XM_011521870.1:c.645C>G XP_011520172.1:p.Leu215=
XM_011521871.1:c.570C>G XP_011520173.1:p.Leu190=
XM_011521872.1:c.570C>G XP_011520174.1:p.Leu190=
XM_011521870.2:c.645C>G XP_011520172.1:p.Leu215=
XM_017022460.1:c.672C>G XP_016877949.1:p.Leu224=
NM_000326.5:c.645C>G MANE Select NP_000317.1:p.Leu215=