Canonical Allele Identifier: CA170835
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 156324
ClinVar RCV Id: RCV000144408
dbSNP Id: rs78340021
MyVariant Identifiers: chr4:g.74277801G>T (hg19) chr4:g.73412084G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73412084G>T , CM000666.2:g.73412084G>T GRCh38
NC_000004.11:g.74277801G>T , CM000666.1:g.74277801G>T GRCh37
NC_000004.10:g.74496665G>T NCBI36
NG_009291.1:g.12830G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.802G>T MANE Select ENSP00000295897.4:p.Glu268Ter
ENST00000295897.8:c.802G>T ENSP00000295897.4:p.Glu268Ter
ENST00000401494.7:c.457G>T ENSP00000384695.3:p.Glu153Ter
ENST00000415165.6:c.226G>T ENSP00000401820.2:p.Glu76Ter
ENST00000476441.6:c.*81G>T ENSP00000423727.1:n.*81G>T
ENST00000503124.5:c.352G>T ENSP00000421027.1:p.Glu118Ter
ENST00000505649.5:n.488G>T
ENST00000507673.1:n.119G>T
ENST00000509063.5:c.802G>T ENSP00000422784.1:p.Glu268Ter
ENST00000511370.1:c.335G>T
ENST00000621085.4:c.490+2722G>T ENSP00000483421.1:n.490+2722G>T
ENST00000621628.4:c.486+3008G>T ENSP00000480485.1:n.486+3008G>T
NM_000477.5:c.802G>T NP_000468.1:p.Glu268Ter
NM_000477.6:c.802G>T NP_000468.1:p.Glu268Ter
NM_000477.7:c.802G>T MANE Select NP_000468.1:p.Glu268Ter
Search 100 bp 5'
Search 100 bp 3'