Canonical Allele Identifier: CA99707196

Gene: ALB

Linked Data

• dbSNP Id: rs866262847
• MyVariant Identifiers: chr4:g.74280781C>T (hg19) ; chr4:g.73415064C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415064C>T , CM000666.2:g.73415064C>T	GRCh38
NC_000004.11:g.74280781C>T , CM000666.1:g.74280781C>T	GRCh37
NC_000004.10:g.74499645C>T	NCBI36
NG_009291.1:g.15810C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1088C>T MANE Select	ENSP00000295897.4:p.Pro363Leu
ENST00000295897.8:c.1088C>T	ENSP00000295897.4:p.Pro363Leu
ENST00000401494.7:c.743C>T	ENSP00000384695.3:p.Pro248Leu
ENST00000415165.6:c.512C>T	ENSP00000401820.2:p.Pro171Leu
ENST00000476441.6:c.*367C>T	ENSP00000423727.1:n.*367C>T
ENST00000484992.1:n.408C>T
ENST00000503124.5:c.638C>T	ENSP00000421027.1:p.Pro213Leu
ENST00000504043.1:n.91C>T
ENST00000505649.5:n.774C>T
ENST00000509063.5:c.1088C>T	ENSP00000422784.1:p.Pro363Leu
ENST00000511370.1:c.621C>T
ENST00000621085.4:c.491-42C>T	ENSP00000483421.1:n.491-42C>T
ENST00000621628.4:c.487-38C>T	ENSP00000480485.1:n.487-38C>T
NM_000477.5:c.1088C>T	NP_000468.1:p.Pro363Leu
NM_000477.6:c.1088C>T	NP_000468.1:p.Pro363Leu
NM_000477.7:c.1088C>T MANE Select	NP_000468.1:p.Pro363Leu